The efficacy of complete blood count parameters in the diagnosis of tubal ectopic pregnancy

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(1)Ginekol Pol. 2014, 85, 823-827. P R A C E. O R Y G I N A L N E po ł o ż n i c t wo. The efficacy of complete blood count parameters in the diagnosis of tubal ectopic pregnancy Skuteczność oznaczania parametrów morfologii w diagnostyce ciąży ektopowej jajowodowej )DWPD(VNLFLR÷OXï$OSHU7XQJDg]GHPLUð*O]DU$U]X7XUDQñ(VUD%DKDU*Uñ (VLQ.DVDSñ0LQH*HQoñ 1. Celal Bayar University, School of Medicine, Department of Obstetrics and Gynecology, Manisa, Turkey ² Ege University, Institute of Health Sciences, Department of Stem Cell, Izmir, Turkey ³ Şifa University, School of Medicine, Department of Obstetrics and Gynecology, Izmir, Turkey. Abstract Objective: Ectopic pregnancy (EP) is the major cause of maternal morbidity and is responsible for maternal mortality in the first trimester. In order to reduce undesirable results, it is necessary to find rapid and accurate, non-surgical diagnostic tests for EP. The goal of the study was to investigate the differences in complete blood count parameters between tubal EPs and healthy pregnancies in be used in the diagnosis of ectopic pregnancy. Study design: White blood cell (WBC), neutrophil, monocyte, lymphocyte, platelet (PLT) counts, mean PLT volume (MPV) and PLT distribution width (PDW) levels in the complete blood count samples have been obtained from subjects with diagnosed tubal EP (n=78; study group) and women with healthy intrauterine gestations (n=79; control group). Statistical comparisons between groups were performed using the t test. Results: PDW levels were found to be significantly higher in the control group than EP (p<0.001). However, no differences between the study and control groups with regard to PLT and MPV levels were observed. WBC levels were found to be significantly higher in the EP group as compared to controls (p<0.001). When leukocyte differentials were compared, monocyte counts in the EP group were significantly higher than in controls (p=0.005). No statistically significant differences in neutrophil and lymphocyte values were observed in either group. Conclusion: PDW as an indicator of PLT activation is lower in tubal EP than intrauterine pregnancy so, possibly, endometrial invasion in the intrauterine pregnancy needs more PLT activation. Monocyte counts are higher in tubal EP, indicating that monocyte activation in the pathophysiology of EP could be effective in the formation of tubal motility and microenvironment regulation.. Key words: ectopic pregnancy / monocyte / platelet activation / leukocyte count /. Address for correspondence: Fatma Eskicioğlu Dept. Of Ob&Gyn, Medical Faculty of Celal Bayar University, Manisa, Turkey 45050 Tel: +90(505)2595349 Fax:+90(236)2327462 e-mail: fatmaeskicioglu@gmail.com. Nr 11/2014. © Polskie Towarzystwo Ginekologiczne. Otrzymano: 26.02.2014 Zaakceptowano do druku: 25.07.2014. 823.

(2) Ginekol Pol. 2014, 85, 823-827. P R A C E O R Y G I N A L N E poł ożn i ct wo. Fatma Eskicioğlu et al. The efficacy of complete blood count parameters in the diagnosis of tubal ectopic pregnancy.. Streszczenie Cel: Ciąża ektopowa (EP) jest główną przyczyną śmiertelności matek w pierwszym trymestrze ciąży. Aby zmniejszyć niekorzystne wyniki tej choroby, konieczne jest znalezienie szybkiego i właściwego testu nieoperacyjnego służącego do rozpoznania EP. Celem badania była ocena różnic w wynikach morfologii pomiędzy pacjentkami z ciążą ektopową a zdrowymi ciężarnymi. Materiał i metoda: W próbkach pełnej krwi zbadano następujące parametry: leukocyty (WBC), neutrofile, monocyty, limfocyty, płytki krwi (PLT), średnią objętość płytki krwi (MPV), szerokość rozdziału płytek (PDW) u pacjentek z rozpoznaną ciążą jajowodową (n=78, grupa badana) oraz u zdrowych ciężarnych (n=79, grupa kontrolna). Analiza statystyczna porównująca obie grupy została wykonana przy pomocy testu t. Wyniki: PDW był istotnie wyższy w grupie kontrolnej niż w grupie EP (p<0,001). Jednak nie znaleziono różnic pomiędzy grupą badaną a kontrolną w odniesieniu do PLT i MPV. WBC było istotnie wyższe w grupie z EP niż w grupie kontrolnej (p<0,001). Odsetek monocytów był istotnie wyższy w grupie EP niż w grupie kontrolnej (p=0,005). Nie obserwowano istotnych różnic w odniesieniu do neutrofili i limfocytów w obu grupach. Wnioski: PDW jako wskaźnik aktywacji płytek krwi jest niższy w ciąży ektopowej niż w ciąży wewnątrzmacicznej, gdyż prawdopodobnie inwazja ciąży w endometrium wymaga większej aktywacji PLT. Odsetek monocytów jest wyższy w ciąży jajowodowej co wskazuje na udział monocytów w procesie patofizjologicznym ciąży ektopowej, w perystaltyce jajowodu i regulacji jego mikrośrodowiska.. Słowa kluczowe:

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(23) PLJKWLQFUHDVHVWKHYHORFLW\DQGSUHFLVLRQ RIWKHGLDJQRVWLFSURFHVVKDVQRWEHHQLGHQWL¿HG\HW>@. Table I. Demographic data in ectopic pregnancy (EP) and control groups (mean±SD, Standard Deviation). Age. EP (n=78). Control (n=79). P value. 30.65±6.07. 26.39±6.21. <0.001. Gravidity. 3.47±1.96. 1.88±1.42. <0.001. Parity. 1.55±1.35. 0.65±0.97. <0.001. Abortions. 0.69±1.04. 0.22±0.65. 0.001. Living children. 2.12±5.96. 0.54±0.93. 0.022. Table II. Platelet (PLT), mean platelet volume (MPV), platelet distribution width (PDW) white blood cell (WBC), neutrophil, monocyte and lymphocyte levels in ectopic pregnancy (EP) and control groups (mean±SD, Standard Deviation). PLT (K/uL). EP (n=78). Control (n=79). P value. 256.64±92.11. 270.58±62.92. 0.269. MPV (fL). 8.38±0.97. 8.69±1.14. 0.79. PDW. 11.55±1.78. 16.36±3.00. <0.001. WBC (K/uL). 11.53±5.18. 8.39±1.66. <0.001. Neutrophil (uL). 7.73±4.74. 5.88±7.36. 0.064. Monocyte (uL). 1.38±0.95. 0.90±1.15. 0.005. Lymphocyte (uL). 2.42±0.69. 2.25±0.62. 0.14. Nr 11/2014. © Polskie Towarzystwo Ginekologiczne. 825.

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(29) Ginekol Pol. 2014, 85, 823-827. P R A C E. O R Y G I N A L N E po ł o ż n i c t wo. Fatma Eskicioğlu et al. The efficacy of complete blood count parameters in the diagnosis of tubal ectopic pregnancy.. 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Source of financing: None. ³. >RO\O S] XY mMYX»SM^ YP SXÔ\O]^]p aRSMR YMM_\] aROX ^RO K_^RY\ \OWKSX] SX. a financial or personal relationship which unjustly affects his/her actions associated with the publication of the manuscript. ³. =Y_\MO YP ºXKXMSXQ$. >RO K_^RY\] \OMOSÒN XY ºXKXMSKV ]_ZZY\^ PY\ ^RO. research, authorship, and/or publication of this article.. References 1. Sivalingam VN, Duncan WC, Kirk E, [et al.]. Diagnosis and management of ectopic pregnancy. J Fam Plann Reprod Health Care. 2011, 37 (4), 231-240. 2. Orazulike NC, Konje JC. Diagnosis and management of ectopic pregnancy. Women’s Health (Lond Engl). 2013, 9 (4), 373-385. 3. Rausch ME, Barnhart KT. Serum biomarkers for detecting ectopic pregnancy. Clin Obstet Gynecol. 2012, 55 (2), 418-423. 4. Pitkin RM, Witte DL. Platelet and leukocyte counts in pregnancy. JAMA. 1979, 242 (24), 26962698. 5. Järemo P, Lindahl TL, Lennmarken C, Forsgren H. The use of platelet density and volume measurements to estimate the severity of pre-eclampsia. Eur J Clin Invest. 2000, 30 (12), 11131118. 6. Vagdatli E, Gounari E, Lazaridou E, [et al.]. Platelet distribution width: a simple, practical and specific marker of activation of coagulation. Hippokratia. 2010, 14 (1), 28-32. 7. Canzoneri BJ, Lewis DF, Groome L, Wang Y. Increased neutrophil numbers account for leukocytosis in women with preeclampsia. Am J Perinatol. 2009, 26 (10), 729-732. 8. Rosevear SK, Liggins GC. Platelet dimensions in pregnancy-induced hypertension. N Z Med J. 1986, 99 (802), 356-357. 9. Turgut A, Sak ME, Ozler A, [et al.]. Alteration of peripheral blood cells in tubal ectopic pregnancy. Ginekol Pol. 2013, 84 (3), 193-196. 10. Barnhart KT. Clinical practice. Ectopic pregnancy. N Engl J Med. 2009, 361, 379–387. 11. Bachman EA, Barnhart K. Medical management of ectopic pregnancy: a comparison of regimens. Clin Obstet Gynecol. 2012, 55 (2), 440-447. 12. Cartwright J, Duncan WC, Critchley HO, [et al.]. Serum biomarkers of tubal ectopic pregnancy: current candidates and future possibilities. Reproduction. 2009, 138, 9–22. 13. Ceyhan T, Beyan C, Başer I, [et al.]. The effect of pre-eclampsia on complete blood count, platelet count and mean platelet volume. Ann Hematol. 2006, 85 (5), 320-322. 14. Taylor DJ, Phillips P, Lind T. Puerperal hematological indices. Br J Obstet Gynaecol. 1981, 88 (6), 601-606.. Authors’ Contribution: 1. Fatma Eskicioğlu – concept, study design, acquisition of data, analysis and interpretation of data, article draft, writing article, corresponding author. 2. Alper Tunga Özdemir – concept, article draft, study design, acquisition of data, revised article critically. 3. Gülüzar Arzu Turan – analysis and interpretation of data, writing article, revised article critically. 4. Esra Bahar Gür – revised article critically, writing article. 5. Esin Kasap – revised article critically. 6. Mine Genç – revised article critically. Authors’ statement ³ This is to certify, that the publication will not violate the copyrights of a third party, as understood according to the Act in the matter of copyright and related rights of 14 February 1994, Official Journal 2006, No. 90, Clause 63, with respect to the text, data, tables and illustrations (graphs, figures, photographs); ³ ^RO\O S] XY mMYX»SM^ YP SXÔ\O]^]p aRSMR YMM_\] aROX ^RO K_^RY\ \OWKSX] SX. a financial or personal relationship which unjustly affects his/her actions associated with the publication of the manuscript; ³ any possible relationship(s) of the author(s) with the party/parties interested in the publication of the manuscript are revealed in the text of the article; ³ the manuscript has not been published in or submitted to any other journal.. Nr 11/2014. 15. Gearing AJ, Hemingway I, Pigott R, [et al.]. Soluble forms of vascular adhesion molecules, E-selectin, ICAM-1, and VCAM-1: pathological significance. Ann N Y Acad Sci. 1992, 667, 324-331. 16. Johnson PM, Christmas SE, Vince GS. Immunological aspects of implantation and implantation failure. Hum Reprod. 1999,14 Suppl 2, 26-36. 17. Shaw JL, Dey SK, Critchley HO, Horne AW. Current knowledge of the aetiology of human tubal ectopic pregnancy. Hum Reprod Update. 2010, 16 (4), 432-444. 18. Rausch ME, Barnhart KT. Serum biomarkers for detecting ectopic pregnancy. Clin Obstet Gynecol. 2012, 55 (2), 418-423. 19. Khatami S, Brummer E, Stevens DA. Effects of granulocyte-macrophage colony stimulating factor (GM-CSF) in vivo on cytokine production and proliferation by spleen cells. Clin Exp Immunol. 2001,125 (2), 198-201. 20. Tonello A, Poli G. Tubal ectopic pregnancy: macrophages under the microscope. Hum Reprod. 2007, 22 (10), 2577-2584. 21. Edelstam G, Löwbeer C, Kral G, [et al.]. New reference values for routine blood samples and human neutrophilic lipocalin during third-trimester pregnancy. Scand J Clin Lab Invest. 2001, 61 (8), 583-592. 22. Sato Y, Fujiwara H, Konishi I. Role of platelets in placentation. Med Mol Morphol. 2010, 43 (3), 129-133. 23. Harper MJ. Platelet-activating factor: a paracrine factor in preimplantation stages of reproduction? Biol Reprod. 1989, 40 (5), 907-913. 24. Saito S. Cytokine cross-talk between mother and the embryo/placenta. J Reprod Immunol. 2001, 52 (1-2), 15–33. 25. Goffin F, Munaut C, Malassiné A, [et al.]. Evidence of a limited contribution of feto-maternal interactions to trophoblast differentiation along the invasive pathway. Tissue Antigens. 2003, 62 (2), 104-116.. © Polskie Towarzystwo Ginekologiczne. 827.

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